NEET PG & INI-CET - Pre-Clinical Sciences (Anatomy, Physiology & Biochemistry)

Clinical Biochemistry & Nutrition question bank (Medical Biochemistry)

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Q1.

In clinical evaluation regarding deficiency in von gierke disease (glycogen storage disease type i) (Case Vignette #1): Which of the following observations or mechanisms is most accurate?

(A)

Lysosomal alpha-1,4-glucosidase deficiency (Pompe disease)

(B)

Glucose-6-Phosphatase deficiency causing fasting hypoglycemia, lactic acidosis, and hepatomegaly

(C)

Branching enzyme deficiency (Andersen disease)

(D)

Muscle glycogen phosphorylase deficiency (McArdle disease)

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Q2.

In clinical evaluation regarding deficiency in von gierke disease (glycogen storage disease type i) (Case Vignette #3): Which of the following observations or mechanisms is most accurate?

(A)

Branching enzyme deficiency (Andersen disease)

(B)

Muscle glycogen phosphorylase deficiency (McArdle disease)

(C)

Glucose-6-Phosphatase deficiency causing fasting hypoglycemia, lactic acidosis, and hepatomegaly

(D)

Lysosomal alpha-1,4-glucosidase deficiency (Pompe disease)

Show answer & solution

Verified Answer & Solution Locked

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